HGVS | Genome Assembly |
---|---|
NC_000010.11:g.43077062T>A , CM000672.2:g.43077062T>A | GRCh38 |
NC_000010.10:g.43572510T>A , CM000672.1:g.43572510T>A | GRCh37 |
NC_000010.9:g.42892516T>A | NCBI36 |
NG_007489.1:g.4994T>A , LRG_518:g.4994T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355710.7:c.-197T>A | ENSP00000347942.3:n.-197T>A | |
XM_011540027.1:c.-197T>A | XP_011538329.1:n.-197T>A | |
NM_020630.5:c.-197T>A | NP_065681.1:n.-197T>A | |
NM_020975.5:c.-197T>A | NP_066124.1:n.-197T>A |